applied 431a automatic peptide synthesizer (Thermo Fisher)
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applied 431a automatic peptide synthesizer
Applied 431a Automatic Peptide Synthesizer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/applied+431a+automatic+peptide+synthesizer/pm20823918-135-13-11
Average 90 stars, based on 1 article reviews
Applied 431a Automatic Peptide Synthesizer, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/applied+431a+automatic+peptide+synthesizer/pm20823918-135-13-11
Average 90 stars, based on 1 article reviews
applied 431a automatic peptide synthesizer - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: Antimicrobial activity and conformation of gaegurin-6 amide and its analogs. Article Snippet: LEE, K.-H., S.-Y.. HONG, J.-E. OH, B.-J.. LEE AND B.-S. CHOI. Article Title: Folding of the presequence of yeast pAPI into an amphipathic helix determines transport of the protein from the cytosol to the vacuole. Article Snippet: 0022±2836/97/151124±15 $25.00/0/mb9 To investigate the role of the 17 residues long presequence (p17) in the transport of the precursor of yeast API (pAPI) from the cytosol to the vacuole we have studied the effects of point mutations upon its conformation and on the process of transport.. H NMR analysis of p17 indicates that in aqueous solution 26% of the molecules have the 4-12 segment folded into an helix.. The hydrophobic environment provided by SDS micelles promotes the folding of 54% of the p17 molecules into a 516 amphipathic a-helix. Synthesized:Article Title: [Peptide inhibitors of myosin light chain kinase. Development of peptidase resistant analogues]. Article Snippet: Myosin light chain kinase (MLCK) is a key regulator of various forms of cellular mobility, in par ticular, endothelial and epithelial permeability.. The membrane penetrative peptide (H RKKYKYRRK NH2, L PIK) is one of the potential MLCK inhibitors for use in humans.. Five analogs of L PIK were syn thesized by the solid phase method of peptide synthesis using Fmoc technology. Article Title: Inhibition of migration of monocytes and granulocytes in vivo by the peptide corresponding to sequence 65-76 of monocyte chemotactic protein-1 (MCP-1). Article Snippet: 339 Chemokines, chemotactic cytokines that regulate migration of inflammation cells such as granulocytes, monocytes, and lymphocytes, are involved in the development of inflammation [1].. It has been hypothesized that inflammation may be one of the causes of atherogenesis [2].. Exacerbation of atherosclerosis, which, as is known from clinical practice, is developed during ischemic heart disease and accompanied by unstable angina pectoris and acute coronary syndrome, is likewise determined by inflammation. Article Title: In vitro activities of native and designed peptide antibiotics against drug sensitive and resistant tumor cell lines. Article Snippet: In order to develop peptide agents with reduced length and enhanced tumoricidal activity, we have designed gaegurin 6 (GGN6) derivatives through deletions and/or substitutions of amino acids.. The deletion of hydrophobic amino terminal region completely abolished antitumor activity whereas the deletion of carboxy terminal region had little influence on antitumor activity.. Antitumor activity of the PTP peptides did not correlate with antibacterial activity. Article Title: Synergistic inhibitory effect of cationic peptides and antimicrobial agents on the growth of oral streptococci. Article Snippet: Although chlorhexidine is one of the most efficacious antimicrobial agents used for the prevention of dental caries, side effects limit its application.. The effects of gaegurin 6 (GGN6), an animal-derived cationic peptide, and its derivatives PTP6 and PTP12 on the growth of oral streptococci were investigated to assess the potential of these agents for use in the prevention of dental caries.. The minimal inhibitory concentrations of the peptides for inhibition of the growth of oral streptococci (Streptococcus mutans, S. sobrinus, S. sanguis and S. gordonii) ranged from 1.2 to 8.2 ÌM. |